Search arXivSearch

arXiv · 2203.06392

A theory for the flow of chemically-responsive polymer solutions: equilibrium and shear-induced phase separation

Abstract

Chemically-responsive polymers are macromolecules that respond to local variations of the chemical composition of the solution by changing their conformation, with notable examples including polyelectrolytes, proteins and DNA. The polymer conformation changes can occur in response to changes to the pH, the ionic strength or to the concentration of a generic solute that interacts with the polymer. These chemical stimuli can lead to drastic variations of the polymer flexibility and even trigger a transition from a coil to a globule polymer conformation. In many situations the spatial distribution of the chemical stimuli can be highly inhomogeneous, which can lead to large spatial variations of polymer conformation and of the rheological properties of the mixture. In this paper, we develop a theory for the flow of a mixture of a solute and chemically-responsive polymers. The approach is valid for generic flows and inhomogeneous distributions of polymers and solutes. To model the polymer conformation changes introduced by the interactions with the solute, we consider the polymers as linear elastic dumbbells whose spring stiffness depends on the solute concentration. We use the Onsager's variational formalism to derive the equations governing the evolution of the variables, which unveils novel couplings between the distribution of dumbbells and that of the solute. Finally, we use a linear stability analysis to show that the governing equations predict an equilibrium phase separation and a distinct shear-induced phase separation whereby a homogeneous distribution of solute and dumbbells spontaneously demix. Similar phase transitions have been observed in previous experiments using stimuli-responsive polymers and may play an important role in living systems.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Marco De Corato, Marino Arroyo. 2022-05-31. A theory for the flow of chemically-responsive polymer solutions: equilibrium and shear-induced phase separation. https://doi.org/10.1122/8.0000475

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Spontaneous Vortex Instability in Active Nematics

One of the defining results in the study of active matter is the spontaneous flow instability, through which a homogeneous, uniformly aligned state breaks translational symmetry along a single direction and develops sustained flow. The vortex state that emerges at higher activity has instead been attributed to nonlinear dynamics. Using a Floquet-type linear stability analysis, we show that no such mechanism is required: the flowing state undergoes a secondary, zigzag instability that breaks the remaining translational symmetry and produces the vortex state. We further identify a regime in which the flowing state ceases to exist and vortices emerge directly from the uniformly aligned state. Under channel confinement, the instability selects a length scale that differs from the establishedactivelengthscale, andsetsthenumberofvorticesthatappear, leadingtoaconfinement- selected pattern reminiscent of a vortex lattice, opening a route toward direct experimental tests of this instability. Full nonlinear simulations reproduce the predicted onset activities and the selected vortex number.

cond-mat.soft

Active pistons extract work by periodic compression alone

Active matter is liable to invent protocols that evade the constraints of equilibrium thermodynamics. We put forward active pistons that extract work by periodic compression alone without changing any bulk property of the system. Such pistons necessarily couple the perturbation imposed by an external operator with some degrees of freedom internal to active components. We illustrate this design principle with elastic networks composed of self-aligning motile particles. For slow protocols, self-alignment always overwhelms mechanical friction when the internal activity exceeds a specific threshold controlled by fluctuations. We identify the key response coefficient that helps delineate regimes of work extraction, and reveal that the corresponding phase diagram follows a master curve with re-entrance in terms of noise amplitude. Overall, our active pistons embody a novel design principle with broad implications for building innovative engines far from equilibrium.

cond-mat.soft

Geometry-induced flocking and topological sound on a defect-free curved surface

We study an ordered polar active flock on a torus and show that topological sound persists on a compact curved surface without topological defects or physical boundaries. Using the covariant Toner Tu theory, we derive an effective nonHermitian Dirac operator whose curvature-induced mass changes sign across the outer and inner equators, producing two Jackiw Rebbi domain walls. These support co-propagating but distinct chiral edge excitations: a density mode localized on the positively curved outer equator and a Goldstone mode localized on the negatively curved inner equator. The bulk bands possess opposite half-integer Chern numbers whose jumps across the domain walls are determined by the sign of the Gaussian curvature. We further show that the localised modes are protected by a one-dimensional Callias index theorem, while the sum of the local indices obeys the Poincare Hopf theorem on the compact surface. Our results establish that curvature alone, independent of defects and boundaries, is sufficient to generate and protect topological sound in active matter, providing a unified connection between non-Hermitian topology, differential geometry, and hydrodynamic theory of collective motion.

cond-mat.soft